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Qualaquin
Qualaquin - 13310-153-07 - (Quinine Sulfate)
Drug Information of Qualaquin
| Product NDC: | 13310-153 |
| Proprietary Name: | Qualaquin |
| Non Proprietary Name: | Quinine Sulfate |
| Active Ingredient(s): | 324 mg/1 & nbsp; Quinine Sulfate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Qualaquin
| Product NDC: | 13310-153 |
| Labeler Name: | AR Scientific Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021799 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20050812 |
Package Information of Qualaquin
| Package NDC: | 13310-153-07 |
| Package Description: | 30 CAPSULE in 1 BOTTLE, PLASTIC (13310-153-07) |
NDC Information of Qualaquin
| NDC Code | 13310-153-07 |
| Proprietary Name | Qualaquin |
| Package Description | 30 CAPSULE in 1 BOTTLE, PLASTIC (13310-153-07) |
| Product NDC | 13310-153 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Quinine Sulfate |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20050812 |
| Marketing Category Name | NDA |
| Labeler Name | AR Scientific Inc. |
| Substance Name | QUININE SULFATE |
| Strength Number | 324 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Antimalarial [EPC] |
